Canonical Allele Identifier: PA2826320806
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230159.1:p.Ala607Val
CA402528341
NM_001243230.2:c.1820C>T